Intermediate-Size Patient Population Expanded Access Program for Intravenous Difelikefalin

NCT05031546 · Status: APPROVED_FOR_MARKETING · Type: EXPANDED_ACCESS

Last updated 2022-05-18

No results posted yet for this study

Summary

This is an intermediate-size patient population expanded access protocol for the use of intravenous (IV) difelikefalin for the treatment of moderate-to-severe pruritus associated with chronic kidney disease in adult patients undergoing hemodialysis.

Conditions

  • Uremic Pruritus

Interventions

DRUG

Difelikefalin

IV Difelikefalin 0.5 mcg/kg administered after each dialysis session (3 times/week)

Sponsors & Collaborators

  • Cara Therapeutics, Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05031546 on ClinicalTrials.gov